Genetic testing in familial and young-onset Alzheimer's disease: Mutation spectrum in a Serbian cohort

Neurobiology of Aging

Volumn 33, Issue 7, 2012, Pages 1481.e7-1481.e12

  Dobricic, Valerija ^a   Stefanova, Elka ^a,b   Jankovic, Milena ^b   Gurunlian, Nicole ^c   Novakovic, Ivana ^a,b   Hardy, John ^c   Kostic, Vladimir ^a,b   Guerreiro, Rita ^c  

^a CLINICAL CENTER OF SERBIA   (Serbia)

^b UNIVERSITY OF BELGRADE   (Serbia)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Alzheimer's disease; APP; Mutations; Presenilins; Serbia

Indexed keywords

AMYLOID BETA PROTEIN; AMYLOID PRECURSOR PROTEIN; APOLIPOPROTEIN E; PRESENILIN 1; PRESENILIN 2;

ADULT; AGED; ALLELE; ALZHEIMER DISEASE; APOE GENE; APP GENE; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; EXON; FAMILY HISTORY; FEMALE; GENE; GENE FREQUENCY; GENE FUNCTION; GENE MUTATION; GENETIC CODE; GENETIC IDENTIFICATION; GENETIC SCREENING; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOTE; HUMAN; MALE; MUTATIONAL ANALYSIS; ONSET AGE; PRIORITY JOURNAL; PSEN1 GENE; PSEN2 GENE; SERBIA; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84861185819     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2011.12.007     Document Type: Article

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